ES2235913T3 - Utilizacion de antiinductores de receptores de gabab y de sus derivados aceptables farmaceuticamente, en la terapia de mantenimiento de la abstinencia de nicotina en pacientes dependientes de la nicotina. - Google Patents
Utilizacion de antiinductores de receptores de gabab y de sus derivados aceptables farmaceuticamente, en la terapia de mantenimiento de la abstinencia de nicotina en pacientes dependientes de la nicotina.Info
- Publication number
- ES2235913T3 ES2235913T3 ES00947901T ES00947901T ES2235913T3 ES 2235913 T3 ES2235913 T3 ES 2235913T3 ES 00947901 T ES00947901 T ES 00947901T ES 00947901 T ES00947901 T ES 00947901T ES 2235913 T3 ES2235913 T3 ES 2235913T3
- Authority
- ES
- Spain
- Prior art keywords
- nicotine
- gaba
- use according
- transcutaneous
- baclofen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 title claims abstract description 48
- 229960002715 nicotine Drugs 0.000 title claims abstract description 47
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 title claims abstract description 45
- 230000001419 dependent effect Effects 0.000 title claims abstract description 7
- 238000009115 maintenance therapy Methods 0.000 title description 2
- 239000000411 inducer Substances 0.000 claims abstract description 13
- 239000000779 smoke Substances 0.000 claims abstract description 9
- 238000011282 treatment Methods 0.000 claims abstract description 9
- 230000009467 reduction Effects 0.000 claims abstract description 7
- 238000002360 preparation method Methods 0.000 claims abstract description 6
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract 3
- KPYSYYIEGFHWSV-UHFFFAOYSA-N Baclofen Chemical compound OC(=O)CC(CN)C1=CC=C(Cl)C=C1 KPYSYYIEGFHWSV-UHFFFAOYSA-N 0.000 claims description 19
- 229960000794 baclofen Drugs 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000003814 drug Substances 0.000 claims description 9
- 229940079593 drug Drugs 0.000 claims description 7
- 102000005962 receptors Human genes 0.000 claims description 7
- 108020003175 receptors Proteins 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 102000017934 GABA-B receptor Human genes 0.000 claims description 5
- 108060003377 GABA-B receptor Proteins 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000006187 pill Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- -1 (methyl) phosphinic acid 3-amino-propyl phosphine Chemical compound 0.000 claims description 4
- 238000009472 formulation Methods 0.000 claims description 4
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- 239000012458 free base Substances 0.000 claims description 2
- 229960003692 gamma aminobutyric acid Drugs 0.000 claims description 2
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 claims description 2
- 238000007918 intramuscular administration Methods 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims description 2
- 239000003405 delayed action preparation Substances 0.000 claims 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 1
- 238000013268 sustained release Methods 0.000 claims 1
- 239000012730 sustained-release form Substances 0.000 claims 1
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical group OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 abstract description 3
- 230000000694 effects Effects 0.000 description 15
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- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 2
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- GVGLGOZIDCSQPN-PVHGPHFFSA-N Heroin Chemical compound O([C@H]1[C@H](C=C[C@H]23)OC(C)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4OC(C)=O GVGLGOZIDCSQPN-PVHGPHFFSA-N 0.000 description 2
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- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 2
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- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
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- PJDFLNIOAUIZSL-UHFFFAOYSA-N vigabatrin Chemical compound C=CC(N)CCC(O)=O PJDFLNIOAUIZSL-UHFFFAOYSA-N 0.000 description 2
- MXYUKLILVYORSK-UHFFFAOYSA-N (+/-)-allo-lobeline Natural products C1CCC(CC(=O)C=2C=CC=CC=2)N(C)C1CC(O)C1=CC=CC=C1 MXYUKLILVYORSK-UHFFFAOYSA-N 0.000 description 1
- MXYUKLILVYORSK-HBMCJLEFSA-N (-)-lobeline Chemical compound C1([C@@H](O)C[C@H]2N([C@H](CCC2)CC(=O)C=2C=CC=CC=2)C)=CC=CC=C1 MXYUKLILVYORSK-HBMCJLEFSA-N 0.000 description 1
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- RTHCYVBBDHJXIQ-MRXNPFEDSA-N (R)-fluoxetine Chemical compound O([C@H](CCNC)C=1C=CC=CC=1)C1=CC=C(C(F)(F)F)C=C1 RTHCYVBBDHJXIQ-MRXNPFEDSA-N 0.000 description 1
- OTABLIMKXCPLGL-UHFFFAOYSA-N 3-phosphanylpropan-1-amine Chemical compound NCCCP OTABLIMKXCPLGL-UHFFFAOYSA-N 0.000 description 1
- MQIWYGZSHIXQIU-UHFFFAOYSA-O 3-phosphopropylazanium Chemical compound NCCC[P+](O)=O MQIWYGZSHIXQIU-UHFFFAOYSA-O 0.000 description 1
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
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- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
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- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/662—Phosphorus acids or esters thereof having P—C bonds, e.g. foscarnet, trichlorfon
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/34—Tobacco-abuse
Landscapes
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Addiction (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT1999MI001715A IT1313585B1 (it) | 1999-07-30 | 1999-07-30 | Uso di agonisti dei recettori gabab per la terapia di mantenimentodell'astinenza da nicotina in soggetti nicotino-dipendenti. |
ITMI991715 | 1999-07-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2235913T3 true ES2235913T3 (es) | 2005-07-16 |
Family
ID=11383467
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES00947901T Expired - Lifetime ES2235913T3 (es) | 1999-07-30 | 2000-06-30 | Utilizacion de antiinductores de receptores de gabab y de sus derivados aceptables farmaceuticamente, en la terapia de mantenimiento de la abstinencia de nicotina en pacientes dependientes de la nicotina. |
Country Status (16)
Country | Link |
---|---|
EP (1) | EP1202727B1 (fr) |
CN (1) | CN1176650C (fr) |
AT (1) | ATE285763T1 (fr) |
AU (1) | AU6153400A (fr) |
CA (1) | CA2379752C (fr) |
DE (1) | DE60017147T2 (fr) |
DK (1) | DK1202727T3 (fr) |
ES (1) | ES2235913T3 (fr) |
HK (1) | HK1046849B (fr) |
IL (2) | IL147876A0 (fr) |
IT (1) | IT1313585B1 (fr) |
PL (1) | PL196334B1 (fr) |
PT (1) | PT1202727E (fr) |
RU (1) | RU2262352C2 (fr) |
SI (1) | SI1202727T1 (fr) |
WO (1) | WO2001008675A1 (fr) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT1660440E (pt) | 2003-08-20 | 2012-05-15 | Xenoport Inc | Pró-fármacos de aciloxialquilcarbamato, métodos de síntese e utilização |
EP2354120A1 (fr) | 2003-08-20 | 2011-08-10 | XenoPort, Inc. | Synthèse de promédicaments a base de carbamate d'acyloxyalkyle et leurs intermédiaires |
US7494985B2 (en) | 2004-11-03 | 2009-02-24 | Xenoport, Inc. | Acyloxyalkyl carbamate prodrugs, methods of synthesis, and use |
WO2006050471A2 (fr) | 2004-11-03 | 2006-05-11 | Xenoport, Inc. | Prodrogues d'acyloxyalkyl carbamate de l'acide 3-aminopropylsulfinique, et procedes de synthese et d'utilisation |
US7585996B2 (en) | 2006-09-15 | 2009-09-08 | Xenoport, Inc. | Acyloxyalkyl carbamate prodrugs, methods of synthesis and use |
JP4498407B2 (ja) | 2006-12-22 | 2010-07-07 | キヤノン株式会社 | プロセスカートリッジ、電子写真画像形成装置、及び、電子写真感光体ドラムユニット |
US7868043B2 (en) | 2008-01-25 | 2011-01-11 | Xenoport, Inc. | Mesophasic forms of (3S)-aminomethyl-5-methyl-hexanoic acid prodrugs and methods of use |
TWI369202B (en) | 2008-01-25 | 2012-08-01 | Xenoport Inc | Enantiomerically resolving acyloxyalkyl thiocarbonates used in synthesizing acyloxyalkyl carbamate prodrugs |
EP2250148B1 (fr) | 2008-01-25 | 2016-08-17 | XenoPort, Inc. | Forme cristalline de sels de calcium d'acide (3s)-aminomethyl-5-methyl-hexanoique et ses procedes d'utilisation |
US7989641B2 (en) | 2008-08-07 | 2011-08-02 | Xenoport, Inc. | Methods of synthesizing N-hydroxysuccinimidyl carbonates |
US8299291B2 (en) | 2008-08-07 | 2012-10-30 | Xenoport, Inc. | Methods of synthesizing 1-(acyloxy)-alkyl carbamate prodrugs |
NZ594648A (en) | 2009-03-03 | 2013-12-20 | Xenoport Inc | Sustained release oral dosage forms of an r-baclofen prodrug |
CA2758245A1 (fr) | 2009-04-17 | 2010-10-21 | Xenoport, Inc. | Derives d'acide gamma-aminobutyrique comme ligands des recepteurs gabab |
WO2011081558A1 (fr) * | 2009-08-21 | 2011-07-07 | Komissarov Jury Vladimirovich | Dispositif pour fumeurs permettant de renoncer à la tabagie |
WO2013023155A1 (fr) | 2011-08-11 | 2013-02-14 | Xenoport, Inc. | Formes cristallines anhydres et hémihydratées d'un promédicament (r)-baclofène, procédés de synthèse et procédés d'utilisation |
AU2019249277A1 (en) * | 2018-04-06 | 2020-10-22 | Ovid Therapeutics Inc. | Use of gaboxadol in the treatment of substance use disorders |
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US4126684A (en) * | 1976-02-11 | 1978-11-21 | Ciba-Geigy Corporation | 4-amino-3-p-halophenylbutyric acids and their derivatives used in the control of narcotic abuse |
US5073539A (en) * | 1990-01-22 | 1991-12-17 | Ciba-Geigy Corporation | Transdermal administration of zwitterionic drugs |
US5760049A (en) * | 1997-02-21 | 1998-06-02 | Synapse Pharmaceuticals International, Inc. | Method for controlling tobacco use and alleviating withdrawal symptoms due to cessation of tobacco use |
US6541520B1 (en) * | 1998-08-05 | 2003-04-01 | Brookhaven Science Associates | Treatment of addiction and addiction-related behavior |
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1999
- 1999-07-30 IT IT1999MI001715A patent/IT1313585B1/it active
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2000
- 2000-06-30 AU AU61534/00A patent/AU6153400A/en not_active Abandoned
- 2000-06-30 SI SI200030632T patent/SI1202727T1/xx unknown
- 2000-06-30 PL PL353373A patent/PL196334B1/pl unknown
- 2000-06-30 EP EP00947901A patent/EP1202727B1/fr not_active Expired - Lifetime
- 2000-06-30 RU RU2002105375/15A patent/RU2262352C2/ru active
- 2000-06-30 CN CNB00811031XA patent/CN1176650C/zh not_active Expired - Lifetime
- 2000-06-30 PT PT00947901T patent/PT1202727E/pt unknown
- 2000-06-30 ES ES00947901T patent/ES2235913T3/es not_active Expired - Lifetime
- 2000-06-30 IL IL14787600A patent/IL147876A0/xx active IP Right Grant
- 2000-06-30 DK DK00947901T patent/DK1202727T3/da active
- 2000-06-30 AT AT00947901T patent/ATE285763T1/de active
- 2000-06-30 CA CA002379752A patent/CA2379752C/fr not_active Expired - Fee Related
- 2000-06-30 DE DE60017147T patent/DE60017147T2/de not_active Expired - Lifetime
- 2000-06-30 WO PCT/EP2000/006120 patent/WO2001008675A1/fr active IP Right Grant
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2002
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- 2002-10-31 HK HK02107911.9A patent/HK1046849B/zh not_active IP Right Cessation
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SI1202727T1 (fr) | 2005-08-31 |
WO2001008675A1 (fr) | 2001-02-08 |
ITMI991715A0 (it) | 1999-07-30 |
ITMI991715A1 (it) | 2001-01-30 |
CN1377265A (zh) | 2002-10-30 |
DK1202727T3 (da) | 2005-05-09 |
EP1202727B1 (fr) | 2004-12-29 |
PL196334B1 (pl) | 2007-12-31 |
RU2262352C2 (ru) | 2005-10-20 |
DE60017147D1 (de) | 2005-02-03 |
PT1202727E (pt) | 2005-05-31 |
CA2379752C (fr) | 2008-05-27 |
HK1046849A1 (en) | 2003-01-30 |
IT1313585B1 (it) | 2002-09-09 |
ATE285763T1 (de) | 2005-01-15 |
PL353373A1 (en) | 2003-11-17 |
CA2379752A1 (fr) | 2001-02-08 |
IL147876A (en) | 2007-06-17 |
AU6153400A (en) | 2001-02-19 |
EP1202727A1 (fr) | 2002-05-08 |
IL147876A0 (en) | 2002-08-14 |
HK1046849B (zh) | 2005-07-15 |
CN1176650C (zh) | 2004-11-24 |
DE60017147T2 (de) | 2006-01-12 |
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